Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia

Biological Psychiatry

Volumn 68, Issue 4, 2010, Pages 320-328

  Pagnamenta, Alistair T ^a   Bacchelli, Elena ^b   De Jonge, Maretha V ^c   Mirza, Ghazala ^a   Scerri, Thomas S ^a   Minopoli, Fiorella ^b   Chiocchetti, Andreas ^d   Ludwig, Kerstin U ^e   Hoffmann, Per ^e   Paracchini, Silvia ^a   Lowy, Ernesto ^a   Harold, Denise H ^f   Chapman, Jade A ^f   Klauck, Sabine M ^d   Poustka, Fritz ^g   Houben, Renske H ^c   Staal, Wouter G ^c   Ophoff, Roel A ^c,h   O'Donovan, Michael C ^f   Williams, Julie ^f   Nthen, Markus M ^e   Schulte Krne, Gerd ⁱ   Deloukas, Panos ^j   Ragoussis, Jiannis ^a   Bailey, Anthony J ^k   Maestrini, Elena ^b   Monaco, Anthony P ^a   more..

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b UNIVERSITY OF BOLOGNA   (Italy)

^c UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^d GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

^e UNIVERSITY OF BONN   (Germany)

^f Cardiff University   (United Kingdom)

^g GOETHE UNIVERSITY   (Germany)

^h UNIVERSITY OF CALIFORNIA   (United States)

ⁱ UNIVERSITY OF MUNICH   (Germany)

^j WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^k WARNEFORD HOSPITAL   (United Kingdom)

more..

Author keywords

Autistic; CNTNAP5; CNV; DOCK4; dyslexia; neurexin

Indexed keywords

CNTNAP5 PROTEIN; DEDICATOR OF CYTOKINESIS 4; IMP2 INNER MITOCHONDRIAL MEMBRANE PROTEASE LIKE PROTEIN; NEUREXIN; PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; AUTISM; BASE PAIRING; CELL JUNCTION; CHROMOSOME 2Q; CHROMOSOME 7Q; CHROMOSOME DELETION; COHORT ANALYSIS; CONTROLLED STUDY; DNA MICROARRAY; DYSLEXIA; EXON; FAMILY; FATHER; GENE AMPLIFICATION; GENE DOSAGE; GENE FUSION; GENE LOCUS; GENE SEQUENCE; GENETIC RISK; GENETIC TRANSCRIPTION; GENOMICS; HUMAN; INHERITANCE; MAJOR CLINICAL STUDY; MISSENSE MUTATION; MOTHER; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; READING; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RISK ASSESSMENT; SCREENING; SEGREGATION ANALYSIS; SIBLING; SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; CASE-CONTROL STUDIES; CELL ADHESION MOLECULES, NEURONAL; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHILD, PRESCHOOL; DNA; DYSLEXIA; FEMALE; GENE EXPRESSION REGULATION; GTPASE-ACTIVATING PROTEINS; HUMANS; MALE; MIDDLE AGED; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; REFERENCE VALUES; SEQUENCE DELETION; SEVERITY OF ILLNESS INDEX; TRANSCRIPTION, GENETIC;

EID: 77955694150     PISSN: 00063223     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biopsych.2010.02.002     Document Type: Article

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